Article

Identification of Novel Gene Variants in Turkish Families with Non-Syndromic Congenital Cataracts Using Whole-Exome Sequencing

2021-12-02

Abstract excerpt

<title>Abstract</title> <p><bold>Purpose </bold>The present study aimed to identify the molecular etiology of non-syndromic congenital cataract (CC) using whole-exome sequencing (WES) analysis. <bold>Methods </bold>In the present study, ophthalmologic results and pedigree analysis of the families of 12 patients with non-syndromic CC were evaluated. WES analysis was conducted after DNA was isolated from peripheral...

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Literature Corpus work: 16862867-32fd-58ce-86ef-511bb853aadc
DOI: 10.21203/rs.3.rs-1072160/v1

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